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Intravenous (IV) infusion is often utilized when continuous and controlled drug delivery is necessary, such as during surgery or in the treatment of chronic diseases. This method offers numerous advantages, including immediate drug action, precise control over dosage, and bypassing the first-pass metabolism.

The one-compartment model for IV infusion uses mathematical equations to describe the rate of change in drug quantity in the body. At steady-state or infusion equilibrium, the drug input equals the drug output, leading to a constant concentration in the body. A semi-logarithmic plot of plasma concentration versus time helps determine the elimination rate constant, k.

In cases where rapid therapeutic concentration is needed, an initial loading dose is administered along with the infusion. The impact of both can be calculated using specific equations. Pharmacokinetic parameters such as volume of distribution (Vd) and half-life (t1/2) can be determined from k, the elimination rate constant, and clearance. These calculations are crucial in dosage regimen design, ensuring effective and safe drug therapy.

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IV InfusionOne compartment ModelDrug DeliveryPharmacokineticsDosage ControlSteady state ConcentrationElimination Rate ConstantLoading DoseVolume Of DistributionHalf lifeDrug TherapyPlasma Concentration

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7.6 : One-Compartment Model: IV Infusion

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7.1 : Analysis Methods of Pharmacokinetic Data: Model and Model-Independent Approaches

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7.2 : Model Approaches for Pharmacokinetic Data: Compartment Models

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7.3 : One-Compartment Open Model for IV Bolus Administration: General Considerations

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7.4 : One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution

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7.5 : One-Compartment Open Model for IV Bolus Administration: Estimation of Clearance

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7.7 : One-Compartment Open Model for Extravascular Administration: Zero-Order Absorption Model

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7.8 : One-Compartment Open Model for Extravascular Administration: First-Order Absorption Model

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7.9 : One-Compartment Open Model: Wagner-Nelson and Loo Riegelman Method for ka Estimation

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7.10 : One-Compartment Open Model: Urinary Excretion Data and Determination of k

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7.11 : Multicompartment Models: Overview

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7.12 : Two-Compartment Open Model: Overview

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7.13 : Two-Compartment Open Model: IV Bolus Administration

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7.14 : Two-Compartment Open Model: IV Infusion

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7.15 : Two-Compartment Open Model: Extravascular Administration

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